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EN 60601-2-23:2015

Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment EN 60601-2-23:2015

Publication date:   Jan 18, 2016

General information

60.60 Standard published   Oct 23, 2015

CENELEC

CLC/TC 62 Electrical equipment in medical practice

European Norm

11.040.55   Diagnostic equipment

Buying

Published

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Scope

IEC 60601-2-23:2011 applies to the basic safety and essential performance of transcutaneous partial pressure monitoring equipment. It applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth. IEC 60601-2-23:2011 does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin (for example conjunctiva, mucosa). This third edition cancels and replaces the second edition published in 1999 and constitutes a technical revision. This edition of IEC 60601-2-23 was revised to align structurally with the 2005 edition of IEC 60601-1.

Related legislation

Legislation related to this standard

93/42/EEC

Medical devices

Legislation 93/42/EEC

Life cycle

PREVIOUSLY

WITHDRAWN
EN 60601-2-23:2000

NOW

PUBLISHED
EN 60601-2-23:2015
60.60 Standard published
Oct 23, 2015

REVISED BY

IN_DEVELOPMENT
prEN IEC 80601-2-23:2024

Relations

Adopted from IEC 60601-2-23:2011 IDENTICAL